Study Data
| Project uploaded by: | Ganesh |
| Project ID: | IMP_100062 |
| Title: | The Quantitative Amino Acid Economy of Yeast Reveals Public versus Private Goods and Guides Syntrophic Community Design |
| Project Description: | Quantitative mass spectrometry based estimates of intra and extracellular amino acids in yeast Quantitative metabolic flux into amino acids using 15N ammonium acetate Quantitative mass spectrometry based amino acid amounts in wild-type and mutant yeast |
| Research Area: | Biological Sciences |
| Funding Source: | DBT Wellcome India Alliance (IA/S/21/2/505922), DBT-DFG Indo-German collaboration grant (IC-12025(22)/4/2023-ICD-DBT) Department of Biotechnology |
| Project Contributors: | Shabbir Ahmad, Ganesh Muthu, Sunil Laxman |
| Sr.No | Sample ID | Sample Name | Organism | Source | Sample Preparation Protocol | Sample Type | Experimental Condition | Time of treatment | Variant/Variety | Gender | Age | Replicates | Storage Conditions | Extraction Protocol | Number of files per sample |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | IMSM_104830 | Fig1_2hour | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in synthetic defined minimal medium over 2-hours. At specific time points, equal numbers of cells (~2x10^7) were rapidly harvested and immediately quenched by plunging them into an extraction buffer of 60% methanol. | Metabolites | Estimates of relative amino acid biosynthetic flux in synthetic medium | NA | NA | NA | NA | 3.0 | NA |
The quenched cells were extracted in 75% ethanol. The mixture was then dried down using a speed vacuum (rotatory evaporator). The dried metabolites were subsequently dissolved in 300 µl of mass spectrometry-grade water, and 10 µl of this sample was injected for targeted LC-MS/MS analysis. |
6.0 |
| 2 | IMSM_104883 | Fig1_4hour | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in synthetic defined minimal medium over 4-hour. At specific time points, equal numbers of cells (~2x10^7) were rapidly harvested and immediately quenched by plunging them into an extraction buffer of 60% methanol. | Metabolites | Estimates of relative amino acid biosynthetic flux in synthetic medium | NA | NA | NA | NA | 3.0 | NA |
The quenched cells were extracted in 75% ethanol. The mixture was then dried down using a speed vacuum (rotatory evaporator). The dried metabolites were subsequently dissolved in 300 µl of mass spectrometry-grade water, and 10 µl of this sample was injected for targeted LC-MS/MS analysis. |
6.0 |
| 3 | IMSM_104884 | Fig1_8hour | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in synthetic defined minimal medium over 8-hours. At specific time points, equal numbers of cells (~2x10^7) were rapidly harvested and immediately quenched by plunging them into an extraction buffer of 60% methanol. | Metabolites | Estimates of relative amino acid biosynthetic flux in synthetic medium | NA | NA | NA | NA | 3.0 | NA |
The quenched cells were extracted in 75% ethanol. The mixture was then dried down using a speed vacuum (rotatory evaporator). The dried metabolites were subsequently dissolved in 300 µl of mass spectrometry-grade water, and 10 µl of this sample was injected for targeted LC-MS/MS analysis. |
6.0 |
| 4 | IMSM_104885 | Fig1_12hour | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in synthetic defined minimal medium over 12-hours. At specific time points, equal numbers of cells (~2x10^7) were rapidly harvested and immediately quenched by plunging them into an extraction buffer of 60% methanol. | Metabolites | Estimates of relative amino acid biosynthetic flux in synthetic medium | NA | NA | NA | NA | 3.0 | NA |
The quenched cells were extracted in 75% ethanol. The mixture was then dried down using a speed vacuum (rotatory evaporator). The dried metabolites were subsequently dissolved in 300 µl of mass spectrometry-grade water, and 10 µl of this sample was injected for targeted LC-MS/MS analysis. |
6.0 |
| 5 | IMSM_104886 | Fig1_24hour | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in synthetic defined minimal medium over 24-hours. At specific time points, equal numbers of cells (~2x10^7) were rapidly harvested and immediately quenched by plunging them into an extraction buffer of 60% methanol. | Metabolites | Estimates of relative amino acid biosynthetic flux in synthetic medium | NA | NA | NA | NA | 3.0 | NA |
The quenched cells were extracted in 75% ethanol. The mixture was then dried down using a speed vacuum (rotatory evaporator). The dried metabolites were subsequently dissolved in 300 µl of mass spectrometry-grade water, and 10 µl of this sample was injected for targeted LC-MS/MS analysis. |
6.0 |
| 6 | IMSM_104887 | Fig2_Ex_2h | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in a minimal medium. At 2hours, 1 ml of culture was collected and centrifuged for 5 minutes at 7000 rpm at room temperature to pellet the cells. Between 250 to 500 µl of the cell-free supernatant was carefully collected for metabolite extraction. | Metabolites | Absolute concentrations of extracellular amino acids (accumulated in the medium) across the indicated times of growth | NA | NA | NA | NA | 3.0 | NA |
The cell-free supernatant was mixed with 75% ethanol to extract extracellular amino acids. The mixture was vortexed for 1.0 minute and placed on ice for a few minutes. Samples were then centrifuged at 16000 rpm for 12 minutes at room temperature. 750 µl of the resulting clear supernatant was transferred to new tubes and dried using a speed vacuum. Dried metabolites were stored at -80°C prior to LC-MS/MS analysis. |
6.0 |
| 7 | IMSM_104888 | Fig2_Ex_4h | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in a minimal medium. At 4hours, 1 ml of culture was collected and centrifuged for 5 minutes at 7000 rpm at room temperature to pellet the cells. Between 250 to 500 µl of the cell-free supernatant was carefully collected for metabolite extraction. | Metabolites | Absolute concentrations of extracellular amino acids (accumulated in the medium) across the indicated times of growth | NA | NA | NA | NA | 3.0 | NA |
The cell-free supernatant was mixed with 75% ethanol to extract extracellular amino acids. The mixture was vortexed for 1.0 minute and placed on ice for a few minutes. Samples were then centrifuged at 16000 rpm for 12 minutes at room temperature. 750 µl of the resulting clear supernatant was transferred to new tubes and dried using a speed vacuum. Dried metabolites were stored at -80°C prior to LC-MS/MS analysis. |
6.0 |
| 8 | IMSM_104889 | Fig2_Ex_8h | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in a minimal medium. At 12hours, 1 ml of culture was collected and centrifuged for 5 minutes at 7000 rpm at room temperature to pellet the cells. Between 250 to 500 µl of the cell-free supernatant was carefully collected for metabolite extraction. | Metabolites | Absolute concentrations of extracellular amino acids (accumulated in the medium) across the indicated times of growth | NA | NA | NA | NA | 3.0 | NA |
The cell-free supernatant was mixed with 75% ethanol to extract extracellular amino acids. The mixture was vortexed for 1.0 minute and placed on ice for a few minutes. Samples were then centrifuged at 16000 rpm for 12 minutes at room temperature. 750 µl of the resulting clear supernatant was transferred to new tubes and dried using a speed vacuum. Dried metabolites were stored at -80°C prior to LC-MS/MS analysis. |
6.0 |
| 9 | IMSM_104890 | Fig2_Ex_12h | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in a minimal medium. At 12hours, 1 ml of culture was collected and centrifuged for 5 minutes at 7000 rpm at room temperature to pellet the cells. Between 250 to 500 µl of the cell-free supernatant was carefully collected for metabolite extraction. | Metabolites | Absolute concentrations of extracellular amino acids (accumulated in the medium) across the indicated times of growth | NA | NA | NA | NA | 3.0 | NA |
The cell-free supernatant was mixed with 75% ethanol to extract extracellular amino acids. The mixture was vortexed for 1.0 minute and placed on ice for a few minutes. Samples were then centrifuged at 16000 rpm for 12 minutes at room temperature. 750 µl of the resulting clear supernatant was transferred to new tubes and dried using a speed vacuum. Dried metabolites were stored at -80°C prior to LC-MS/MS analysis. |
6.0 |
| 10 | IMSM_104891 | Fig2_Ex_24h | Saccharomyces cerevisiae | 4932 | Metabolites from S.cerevisiae cells grown in different conditions | S. cerevisiae cultures were grown in a minimal medium. At 24hours, 1 ml of culture was collected and centrifuged for 5 minutes at 7000 rpm at room temperature to pellet the cells. Between 250 to 500 µl of the cell-free supernatant was carefully collected for metabolite extraction. | Metabolites | Absolute concentrations of extracellular amino acids (accumulated in the medium) across the indicated times of growth | NA | NA | NA | NA | 3.0 | NA |
The cell-free supernatant was mixed with 75% ethanol to extract extracellular amino acids. The mixture was vortexed for 1.0 minute and placed on ice for a few minutes. Samples were then centrifuged at 16000 rpm for 12 minutes at room temperature. 750 µl of the resulting clear supernatant was transferred to new tubes and dried using a speed vacuum. Dried metabolites were stored at -80°C prior to LC-MS/MS analysis. |
6.0 |
| Sr.No | MS Exp ID | Sample Name/ID | Mass Spectrometer Type | MS Instrument Name | MS Instrument type | MS Ionization Method | Ion Mode/Scan Polarity | Data Transformation (Software/s Used) |
|---|---|---|---|---|---|---|---|---|
| 71 | IME_103404 | Fig2_Int_4h / IMSM_104893 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 72 | IME_103405 | Fig2_Int_4h / IMSM_104893 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 73 | IME_103406 | Fig2_Int_8h / IMSM_104894 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 74 | IME_103407 | Fig2_Int_8h / IMSM_104894 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 75 | IME_103408 | Fig2_Int_8h / IMSM_104894 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 76 | IME_103409 | Fig2_Int_8h / IMSM_104894 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 77 | IME_103410 | Fig2_Int_8h / IMSM_104894 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 78 | IME_103411 | Fig2_Int_8h / IMSM_104894 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 79 | IME_103412 | Fig2_Int_12h / IMSM_104895 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| 80 | IME_103413 | Fig2_Int_12h / IMSM_104895 | LCMS (Liquid Chromatography- Mass Spectrometry) | ABI Sciex 5500 QTrap | Triple quadrupole | Electrospray Ionization - ESI | Positive | MultiQuant |
| Sr.No | First name | Last name | Organization | Designation | |
|---|---|---|---|---|---|
| 1 | Sunil | Laxman | sunil@instem.res.in | BRIC inStem | principal_investigator |
| 2 | Ganesh | Muthu | ganeshm@instem.res.in | BRIC inStem | research_scholar |
| 3 | Shabbir | Ahmad | shabbirmd@instem.res.in | BRIC inStem | postdoctoral_researcher |
| Sr.No | ftprun ID | MS Exp ID | MS Data Files |
|---|---|---|---|
| 121 | IMR_104058 | IME_103454 | Fig5_ctrl_12_H_Int_35_mM_A.wiff |
| 122 | IMR_104059 | IME_103455 | Fig5_ctrl_12_H_Int_35_mM_A.wiff.scan |
| 123 | IMR_104060 | IME_103456 | Fig5_ctrl_12_H_Int_35_mM_B.wiff |
| 124 | IMR_104061 | IME_103457 | Fig5_ctrl_12_H_Int_35_mM_B.wiff.scan |
| 125 | IMR_104062 | IME_103458 | Fig5_ctrl_12_H_Int_35_mM_C.wiff |
| 126 | IMR_104063 | IME_103459 | Fig5_ctrl_12_H_Int_35_mM_C.wiff.scan |
| 127 | IMR_104064 | IME_103460 | Fig5_12H_ex_350_uM_A.wiff |
| 128 | IMR_104065 | IME_103461 | Fig5_12H_ex_350_uM_A.wiff.scan |
| 129 | IMR_104066 | IME_103462 | Fig5_12H_ex_350_uM_B.wiff |
| 130 | IMR_104067 | IME_103463 | Fig5_12H_ex_350_uM_B.wiff.scan |